A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951717



Internal ID22727070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185874841..185874841hg38UCSC Ensembl
chr4:186795995..186795995hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421727
Samples
Known GenesSORBS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951717
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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